Canonical Allele Identifier: CA412374478
Gene: PHKA2 HGNC NCBI
PHKA2-AS1 HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000023.11:g.18893600T>A , CM000685.2:g.18893600T>A GRCh38
NC_000023.10:g.18911718T>A , CM000685.1:g.18911718T>A GRCh37
NC_000023.9:g.18821639T>A NCBI36
NG_016622.1:g.95763A>T

Transcript Alleles

HGVS Amino-acid Change
ENST00000379942.5:c.3593A>T (PHKA2) MANE Select ENSP00000369274.4:p.His1198Leu
ENST00000379942.4:c.3593A>T (PHKA2) ENSP00000369274.4:p.His1198Leu
ENST00000469485.5:n.1318A>T (PHKA2)
ENST00000473597.1:n.362A>T (PHKA2)
ENST00000481718.1:n.2487A>T (PHKA2)
NM_000292.2:c.3593A>T (PHKA2) NP_000283.1:p.His1198Leu
NR_029379.1:n.467+262T>A (PHKA2-AS1)
XM_005274548.3:c.3539A>T (PHKA2) XP_005274605.1:p.His1180Leu
XM_005274550.3:c.3509A>T (PHKA2) XP_005274607.1:p.His1170Leu
XM_006724496.2:c.3617A>T (PHKA2) XP_006724559.1:p.His1206Leu
XM_006724498.2:c.3071A>T (PHKA2) XP_006724561.1:p.His1024Leu
XM_011545537.1:c.3518A>T (PHKA2) XP_011543839.1:p.His1173Leu
XM_011545538.1:c.2600A>T (PHKA2) XP_011543840.1:p.His867Leu
XM_005274548.5:c.3539A>T (PHKA2) XP_005274605.1:p.His1180Leu
XM_005274550.5:c.3509A>T (PHKA2) XP_005274607.1:p.His1170Leu
XM_006724496.4:c.3617A>T (PHKA2) XP_006724559.1:p.His1206Leu
XM_006724498.4:c.3071A>T (PHKA2) XP_006724561.1:p.His1024Leu
XM_011545537.3:c.3518A>T (PHKA2) XP_011543839.1:p.His1173Leu
XM_011545538.3:c.2600A>T (PHKA2) XP_011543840.1:p.His867Leu
XM_017029580.2:c.2711A>T (PHKA2) XP_016885069.1:p.His904Leu
XR_001755698.2:n.5721A>T (PHKA2)
NM_000292.3:c.3593A>T (PHKA2) MANE Select NP_000283.1:p.His1198Leu